-
2
-
-
0029070763
-
Pharmaceutical solids: Strategic approach to regulatory considerations
-
Byrn S, Pfeiffer R, Ganey M, Hoiberg C, Poole JW, Poochikian G. 1995. Pharmaceutical solids: Strategic approach to regulatory considerations. Pharm Res 12:945-954.
-
(1995)
Pharm Res
, vol.12
, pp. 945-954
-
-
Byrn, S.1
Pfeiffer, R.2
Ganey, M.3
Hoiberg, C.4
Poole, J.W.5
Poochikian, G.6
-
3
-
-
12444319935
-
Scientific considerations of pharmaceutical solid polymorphism in Abbreviated New Drug Applications
-
Yu LX, Furness MS, Raw A, Woodland Outlaw KP, Nashed NE, Ramos E, Miller SPF, Adams RC, Fang F, Patel RM, Holcombe FO Jr, Chiu Y, Hussain AS. 2003. Scientific considerations of pharmaceutical solid polymorphism in Abbreviated New Drug Applications. Pharm Res 20:531-536.
-
(2003)
Pharm Res
, vol.20
, pp. 531-536
-
-
Yu, L.X.1
Furness, M.S.2
Raw, A.3
Woodland Outlaw, K.P.4
Nashed, N.E.5
Ramos, E.6
Miller, S.P.F.7
Adams, R.C.8
Fang, F.9
Patel, R.M.10
Holcombe Jr., F.O.11
Chiu, Y.12
Hussain, A.S.13
-
4
-
-
0029074760
-
Inferring thermodynamic stability relationship of polymorphs from melting data
-
Yu L. 1995. Inferring thermodynamic stability relationship of polymorphs from melting data. J Pharm Sci 84:966-974.
-
(1995)
J Pharm Sci
, vol.84
, pp. 966-974
-
-
Yu, L.1
-
5
-
-
0034820059
-
Estimating the relative stability of polymorphs and hydrates from heats of solution and solubility data
-
Gu CH, Grant DJ. 2001. Estimating the relative stability of polymorphs and hydrates from heats of solution and solubility data. J Pharm Sci 90: 1277-1287.
-
(2001)
J Pharm Sci
, vol.90
, pp. 1277-1287
-
-
Gu, C.H.1
Grant, D.J.2
-
6
-
-
0014104395
-
Effect of polymorphism on the absorption of chloramphenicol from chlroamphenicol palmtate
-
Aguiar AJ, Krc J, Kinkel AW, Samyn JC. 1967. Effect of polymorphism on the absorption of chloramphenicol from chlroamphenicol palmtate. J Pharm Sci 56:847-853.
-
(1967)
J Pharm Sci
, vol.56
, pp. 847-853
-
-
Aguiar, A.J.1
Krc, J.2
Kinkel, A.W.3
Samyn, J.C.4
-
7
-
-
0016074395
-
Bioavailability determination of two crystal forms of sulfameter in humans from urinary excretion data
-
Khalafallah N, Khalil SA, Moustafa MA. 1974. Bioavailability determination of two crystal forms of sulfameter in humans from urinary excretion data. J Pharm Sci 63:861-864.
-
(1974)
J Pharm Sci
, vol.63
, pp. 861-864
-
-
Khalafallah, N.1
Khalil, S.A.2
Moustafa, M.A.3
-
8
-
-
0019858821
-
Comparative studies on dissolution and the bioavailability of ampicillin anhydrate and trihydrate
-
Ali AA, Farouk A. 1981. Comparative studies on dissolution and the bioavailability of ampicillin anhydrate and trihydrate. Int J Pharm 9:239-243.
-
(1981)
Int J Pharm
, vol.9
, pp. 239-243
-
-
Ali, A.A.1
Farouk, A.2
-
9
-
-
0014562040
-
Dissolution behavior of polymorphs of chloramphenicol palmitate and mefenamic acid
-
Aguiar AJ, Zelmer JE. 1969. Dissolution behavior of polymorphs of chloramphenicol palmitate and mefenamic acid. J Pharm Sci 58:983-987.
-
(1969)
J Pharm Sci
, vol.58
, pp. 983-987
-
-
Aguiar, A.J.1
Zelmer, J.E.2
-
10
-
-
0033756813
-
Statistical properties of thermodynamic quantities for cyclodextrin complex formation
-
Burnette RR, Connors KA. 2000 Statistical properties of thermodynamic quantities for cyclodextrin complex formation. J Pharm Sci 89:1389-1394.
-
(2000)
J Pharm Sci
, vol.89
, pp. 1389-1394
-
-
Burnette, R.R.1
Connors, K.A.2
-
11
-
-
0031473049
-
Characterization and interconversion of polymorphs of premafloxacin, a new quinolone antibiotic
-
Schinzer WC, Bergren MS, Aldrich DS, Chao RS, Dunn MJ, Jeganathan A, Madden LM. 1997. Characterization and interconversion of polymorphs of premafloxacin, a new quinolone antibiotic. J Pharm Sci 86:1426-1431.
-
(1997)
J Pharm Sci
, vol.86
, pp. 1426-1431
-
-
Schinzer, W.C.1
Bergren, M.S.2
Aldrich, D.S.3
Chao, R.S.4
Dunn, M.J.5
Jeganathan, A.6
Madden, L.M.7
-
12
-
-
0033962627
-
Preparation and characterization of a new polymorphic form and a solvate form of glibenclamide
-
Panagopoulou-Kalpani A, Malamatris S. 2000. Preparation and characterization of a new polymorphic form and a solvate form of glibenclamide. Int J Pharm 195:239-245.
-
(2000)
Int J Pharm
, vol.195
, pp. 239-245
-
-
Panagopoulou-Kalpani, A.1
Malamatris, S.2
-
13
-
-
77951689740
-
Dissolution behavior of crystalline solvated and nonsolvated forms of some pharmaceuticals
-
Shefter E, Higuchi T. 1963. Dissolution behavior of crystalline solvated and nonsolvated forms of some pharmaceuticals. J Pharm Sci 52:781-791.
-
(1963)
J Pharm Sci
, vol.52
, pp. 781-791
-
-
Shefter, E.1
Higuchi, T.2
-
14
-
-
0037945704
-
Crystal forms of LY334370 HCl: Isolation, solid-state characterization, and physicochemical properties
-
Reutzel-Edens SM, Kleemann RL, Lewellen PL, Borghese AL, Antoine LJ. 2003 Crystal forms of LY334370 HCl: Isolation, solid-state characterization, and physicochemical properties. J Pharm Sci 92:1196-1205.
-
(2003)
J Pharm Sci
, vol.92
, pp. 1196-1205
-
-
Reutzel-Edens, S.M.1
Kleemann, R.L.2
Lewellen, P.L.3
Borghese, A.L.4
Antoine, L.J.5
-
16
-
-
36849125484
-
Thermodynamic driving force in nucleation and growth processes
-
Hoffman JD. 1958. Thermodynamic driving force in nucleation and growth processes. J Chem Phys 29: 1192-1193.
-
(1958)
J Chem Phys
, vol.29
, pp. 1192-1193
-
-
Hoffman, J.D.1
-
17
-
-
1142303337
-
What is the true solubility advantage for amorphous pharmaceuticals?
-
Hancock BC, Parks M. 2000. What is the true solubility advantage for amorphous pharmaceuticals? Pharm Res 17:397-403.
-
(2000)
Pharm Res
, vol.17
, pp. 397-403
-
-
Hancock, B.C.1
Parks, M.2
-
18
-
-
0028948839
-
A theoretical basis for a biopharmaceutical drug classification: The correlation of in-vitro drug product dissolution and in-vivo bioavailability
-
Amdion GL, Lennernas H, Shah VP, Crison JR. 1995. A theoretical basis for a biopharmaceutical drug classification: The correlation of in-vitro drug product dissolution and in-vivo bioavailability. Pharm Res 12:413-420.
-
(1995)
Pharm Res
, vol.12
, pp. 413-420
-
-
Amdion, G.L.1
Lennernas, H.2
Shah, V.P.3
Crison, J.R.4
-
19
-
-
0001256286
-
Effects of polymorphism and solid-state solvation on solubility and dissolution rate
-
Brittain HG. editor. New York: Marcel Dekker
-
Brittain HG, Grant DJW. 1999. Effects of polymorphism and solid-state solvation on solubility and dissolution rate. In: Brittain HG. editor. Polymorphism in pharmaceutical solids. New York: Marcel Dekker. pp 279-330.
-
(1999)
Polymorphism in Pharmaceutical Solids
, pp. 279-330
-
-
Brittain, H.G.1
Grant, D.J.W.2
-
20
-
-
0027230053
-
Polymorphism and pseudopolymorphism of acemetacin
-
Burger A, Lettenbichler A. 1993. Polymorphism and pseudopolymorphism of acemetacin. Pharmazie 48:262-272.
-
(1993)
Pharmazie
, vol.48
, pp. 262-272
-
-
Burger, A.1
Lettenbichler, A.2
-
21
-
-
0031048775
-
Polymorphic drug substances of the European Pharmacopeia, Part 9: Physicochemical properties and crystal structure of acetazolamide crystal forms
-
Griesser UJ, Burger A, Mereiter K. 1997. Polymorphic drug substances of the European Pharmacopeia, Part 9: Physicochemical properties and crystal structure of acetazolamide crystal forms. J Pharm Sci 86:352-358.
-
(1997)
J Pharm Sci
, vol.86
, pp. 352-358
-
-
Griesser, U.J.1
Burger, A.2
Mereiter, K.3
-
22
-
-
0027263963
-
Relative physical stability of the solid forms of amiloride hydrochloride
-
Jozwiakowski MJ, Williams SO, Hathaway RD. 1995. Relative physical stability of the solid forms of amiloride hydrochloride. Int J Pharm 91:195-207.
-
(1995)
Int J Pharm
, vol.91
, pp. 195-207
-
-
Jozwiakowski, M.J.1
Williams, S.O.2
Hathaway, R.D.3
-
23
-
-
0026496153
-
Potential cardiotonic agents, Part 15: Crystal modifications of 3-cyano-2-morpholino-5-(4-pyridinyl)pyridine (AWD-122-14)
-
Hagen V, Reck G, Dathe M, Jansch HJ, Feist M. 1992. Potential cardiotonic agents, Part 15: Crystal modifications of 3-cyano-2-morpholino-5-(4-pyridinyl) pyridine (AWD-122-14). Pharmazie 47:777-780.
-
(1992)
Pharmazie
, vol.47
, pp. 777-780
-
-
Hagen, V.1
Reck, G.2
Dathe, M.3
Jansch, H.J.4
Feist, M.5
-
24
-
-
0028067103
-
Physicochemical characterization of the various solid forms of carbovir, an antiviral nucleoside
-
Nguyen NA, Ghosh S, Gatlin LA, Grant DJ. 1994. Physicochemical characterization of the various solid forms of carbovir, an antiviral nucleoside. J Pharm Sci 83:1116-1123.
-
(1994)
J Pharm Sci
, vol.83
, pp. 1116-1123
-
-
Nguyen, N.A.1
Ghosh, S.2
Gatlin, L.A.3
Grant, D.J.4
-
25
-
-
0028285929
-
Polymorphsim of diflunisal: Isolation and solid-state characterization of a new crystal form
-
Martinez-Oharriz MC, Martin C, Goni MM, Rodriguez-Espinosa C, Sanchez M. 1994. Polymorphsim of diflunisal: Isolation and solid-state characterization of a new crystal form. J Pharm Sci 83:174-177.
-
(1994)
J Pharm Sci
, vol.83
, pp. 174-177
-
-
Martinez-Oharriz, M.C.1
Martin, C.2
Goni, M.M.3
Rodriguez-Espinosa, C.4
Sanchez, M.5
-
26
-
-
0028242658
-
Spectroscopic investigation of DuP-747 polymorphs
-
Raghavan K, Dwivedi A, Campbell GC, Nemeth G, Hussain MA. 1994. Spectroscopic investigation of DuP-747 polymorphs. J Pharm Biol Med Anal 12:777-785.
-
(1994)
J Pharm Biol Med Anal
, vol.12
, pp. 777-785
-
-
Raghavan, K.1
Dwivedi, A.2
Campbell, G.C.3
Nemeth, G.4
Hussain, M.A.5
-
27
-
-
0036785624
-
Solid state characterization of E2101, a novel antispastic drug
-
Kushida I, Ashizawa K. 2002. Solid state characterization of E2101, a novel antispastic drug. J Pharm Sci 91:2193-2202.
-
(2002)
J Pharm Sci
, vol.91
, pp. 2193-2202
-
-
Kushida, I.1
Ashizawa, K.2
-
28
-
-
0032948684
-
Metastable polymorphs of Etoposide with higher dissolution rate
-
Shah JC, Chen JR, Chow D. 1999. Metastable polymorphs of Etoposide with higher dissolution rate. Drug Dev Ind Pharm 25:63-67.
-
(1999)
Drug Dev Ind Pharm
, vol.25
, pp. 63-67
-
-
Shah, J.C.1
Chen, J.R.2
Chow, D.3
-
29
-
-
0027092645
-
Characterization of polymorphs and solvates of 3-amino-1-(m- trifluoromethylphenyl)-6-methyl-1H-pyridazin-4-one
-
Chauvet A, Masse J, Ribet JP, Bigg D, Austin JM, Patoiseau JF, Jaud J. 1992. Characterization of polymorphs and solvates of 3-amino-1-(m- trifluoromethylphenyl)-6-methyl-1H-pyridazin-4-one. J Pharm Sci. 81:836-841.
-
(1992)
J Pharm Sci
, vol.81
, pp. 836-841
-
-
Chauvet, A.1
Masse, J.2
Ribet, J.P.3
Bigg, D.4
Austin, J.M.5
Patoiseau, J.F.6
Jaud, J.7
-
31
-
-
0034578675
-
Solid-state studies on hemihydrate and the anhydrous forms of flunisolide
-
Bartolomei M. 2000. Solid-state studies on hemihydrate and the anhydrous forms of flunisolide. J Pharm Biomed Anal 24:81-93.
-
(2000)
J Pharm Biomed Anal
, vol.24
, pp. 81-93
-
-
Bartolomei, M.1
-
32
-
-
0015130813
-
Isolation and characterization of solid phases of flurprednisilone
-
Haleblian JK, Koda RT, Biles JA. 1971. Isolation and characterization of solid phases of flurprednisilone. J Pharm Sci 60:1485-1488.
-
(1971)
J Pharm Sci
, vol.60
, pp. 1485-1488
-
-
Haleblian, J.K.1
Koda, R.T.2
Biles, J.A.3
-
33
-
-
0025261002
-
Physicochemical characterization of furosemide modifications
-
Matsuda Y, Tatsumi E. 1990. Physicochemical characterization of furosemide modifications. Int J Pharm 60:11-26.
-
(1990)
Int J Pharm
, vol.60
, pp. 11-26
-
-
Matsuda, Y.1
Tatsumi, E.2
-
35
-
-
0030997813
-
Characterization of polymorphs and hydrates of GK-128, a serotonin3 receptor antagonist
-
Ito S, Nishimura M, Kobayashi Y, Itai S, Yamamoto K. 1997. Characterization of polymorphs and hydrates of GK-128, a serotonin3 receptor antagonist. Int J Pharm 151:133-143.
-
(1997)
Int J Pharm
, vol.151
, pp. 133-143
-
-
Ito, S.1
Nishimura, M.2
Kobayashi, Y.3
Itai, S.4
Yamamoto, K.5
-
36
-
-
0024580170
-
Isolation and physicochemical characterization of solid forms of glibenclamide
-
Suleiman MS, Najib NM. 1989. Isolation and physicochemical characterization of solid forms of glibenclamide. Int J Pharm 50:103-109.
-
(1989)
Int J Pharm
, vol.50
, pp. 103-109
-
-
Suleiman, M.S.1
Najib, N.M.2
-
37
-
-
0032967393
-
Physicochemical characterization of glybuzole polymorphs and their pharmaceutical properties
-
Otsuka M, Ofusa T, Matsuda Y. 1999. Physicochemical characterization of glybuzole polymorphs and their pharmaceutical properties. Drug Dev Ind Pharm 25:197-203.
-
(1999)
Drug Dev Ind Pharm
, vol.25
, pp. 197-203
-
-
Otsuka, M.1
Ofusa, T.2
Matsuda, Y.3
-
38
-
-
0033987197
-
Polymorphism and preformulation studies in lifibrol
-
Burger A, Lettenbichler A. 2000. Polymorphism and preformulation studies in lifibrol. Eur J Pharm Biopharm 49:65-72.
-
(2000)
Eur J Pharm Biopharm
, vol.49
, pp. 65-72
-
-
Burger, A.1
Lettenbichler, A.2
-
39
-
-
0027215218
-
Spectroscopic investigation of losartan polymorphs
-
Raghavan K, Dwivedi A, Campbell GC, Johnston E, Levorse D, McCauley JA, Hussain M. 1993. Spectroscopic Investigation of losartan polymorphs. Pharm Res 10:900-904.
-
(1993)
Pharm Res
, vol.10
, pp. 900-904
-
-
Raghavan, K.1
Dwivedi, A.2
Campbell, G.C.3
Johnston, E.4
Levorse, D.5
McCauley, J.A.6
Hussain, M.7
-
40
-
-
0037331309
-
Developing a discriminating dissolution test for three mebendazole polymorphs based on solubility differences
-
Swanepoel E, Liebenberg W, Dewarakonda B, De Villiers MM. 2003. Developing a discriminating dissolution test for three mebendazole polymorphs based on solubility differences. Pharmazie 58: 117-121.
-
(2003)
Pharmazie
, vol.58
, pp. 117-121
-
-
Swanepoel, E.1
Liebenberg, W.2
Dewarakonda, B.3
De Villiers, M.M.4
-
41
-
-
0000182441
-
Polymorphism and drug availability: Solubility relations in the methylprednisolone system
-
Higuchi WI, Lau PK, Higuchi T, Shell JW. 1963. Polymorphism and drug availability: Solubility relations in the methylprednisolone system. J Pharm Sci 52:150-153.
-
(1963)
J Pharm Sci
, vol.52
, pp. 150-153
-
-
Higuchi, W.I.1
Lau, P.K.2
Higuchi, T.3
Shell, J.W.4
-
42
-
-
0025232683
-
Study of the polymorphism of 3-((3-(2-(7-chloro-2-quinolinyl)-(E)- ethenyl)phenyl)((3-dimethylamino-3 oxopropyl) thio)methyl)-thio)propanoic yl)thio)methyl)-thio)-propanoic acid (MK571) by DSC, TG, XRPD and solubility measurements
-
Ghodbane S, McCauley JA. 1990. Study of the polymorphism of 3-((3-(2-(7-chloro-2-quinolinyl)-(E)-ethenyl)phenyl)((3-dimethylamino-3 oxopropyl) thio)methyl)-thio)propanoic yl)thio)methyl)-thio)-propanoic acid (MK571) by DSC, TG, XRPD and solubility measurements. Int J Pharm 59:281-286.
-
(1990)
Int J Pharm
, vol.59
, pp. 281-286
-
-
Ghodbane, S.1
McCauley, J.A.2
-
43
-
-
0032921265
-
Investigation of the polymorphism of the angiotensin II antagonist agent MK-996
-
Jahansouz H, Thompson KC, Brenner GS, Kauffman MJ. 1999. Investigation of the polymorphism of the angiotensin II antagonist agent MK-996. Pharm Dev Tech 4:181-187.
-
(1999)
Pharm Dev Tech
, vol.4
, pp. 181-187
-
-
Jahansouz, H.1
Thompson, K.C.2
Brenner, G.S.3
Kauffman, M.J.4
-
44
-
-
0027943415
-
Investigation of moricizine hydrochloride polymorphs
-
Wu LS, Torosian G, Sigvardson K, Gerard C, Hussain MA. 1994. Investigation of moricizine hydrochloride polymorphs. J Pharm Sci 83:1404-1406.
-
(1994)
J Pharm Sci
, vol.83
, pp. 1404-1406
-
-
Wu, L.S.1
Torosian, G.2
Sigvardson, K.3
Gerard, C.4
Hussain, M.A.5
-
45
-
-
0347360187
-
Preparation and physicochemical properties of niclosamide anhydrate and two monohydrates
-
van Tonder EC, Maleka TSP, Liebenberg W, Song M, Wurster DE, De Villiers MM. 2004. Preparation and physicochemical properties of niclosamide anhydrate and two monohydrates. Int J Pharm 269:417-432.
-
(2004)
Int J Pharm
, vol.269
, pp. 417-432
-
-
Van Tonder, E.C.1
Maleka, T.S.P.2
Liebenberg, W.3
Song, M.4
Wurster, D.E.5
De Villiers, M.M.6
-
47
-
-
0028791818
-
Dissolution behavior of piretanide polymorphs at various temperatures and pHs
-
Chikaraishi Y, Otsuka M, Matsuda Y. 1995. Dissolution behavior of piretanide polymorphs at various temperatures and pHs. Chem Pharm Bull 43:1966-1969.
-
(1995)
Chem Pharm Bull
, vol.43
, pp. 1966-1969
-
-
Chikaraishi, Y.1
Otsuka, M.2
Matsuda, Y.3
-
48
-
-
0037473468
-
Characterization of piroxicam crystal modifications
-
Vrecer F, Vrbinc M, Meden A. 2003. Characterization of piroxicam crystal modifications. Int J Pharm 256:3-15.
-
(2003)
Int J Pharm
, vol.256
, pp. 3-15
-
-
Vrecer, F.1
Vrbinc, M.2
Meden, A.3
-
49
-
-
0032720026
-
Physicochemical characterization of the modification I and II of (R,S) propranolol hydrochloride: Solubility and dissolution studies
-
Bartolomei M, Bertocchi P, Ramusino MC, Santucci N, Valvo L. 1999. Physicochemical characterization of the modification I and II of (R,S) propranolol hydrochloride: solubility and dissolution studies. J Pharm Biomed Anal 21:299-309.
-
(1999)
J Pharm Biomed Anal
, vol.21
, pp. 299-309
-
-
Bartolomei, M.1
Bertocchi, P.2
Ramusino, M.C.3
Santucci, N.4
Valvo, L.5
-
50
-
-
0028318607
-
Preparation and characterization of ranitidine hydrochloride crystals
-
Madan T, Kakkar AP. 1994. Preparation and characterization of ranitidine hydrochloride crystals. Drug Dev Ind Pharm 20:1571-1588.
-
(1994)
Drug Dev Ind Pharm
, vol.20
, pp. 1571-1588
-
-
Madan, T.1
Kakkar, A.P.2
-
51
-
-
0029876319
-
Preparation and characterization of polymorphs for an LTD4 antagonist, RG 12525
-
Carlton RA, Difeo TJ, Powner TH, Santos I, Thompson MD. 1996. Preparation and characterization of polymorphs for an LTD4 antagonist, RG 12525. J Pharm Sci 85:461-467.
-
(1996)
J Pharm Sci
, vol.85
, pp. 461-467
-
-
Carlton, R.A.1
Difeo, T.J.2
Powner, T.H.3
Santos, I.4
Thompson, M.D.5
-
52
-
-
0034874245
-
Ritonavir: An extrordinary example of conformational polymoprhism
-
Bauer J, Spanton S, Henry R, Quick J, Morris J. 2001. Ritonavir: An extrordinary example of conformational polymoprhism. Pharm Res 18:859-866.
-
(2001)
Pharm Res
, vol.18
, pp. 859-866
-
-
Bauer, J.1
Spanton, S.2
Henry, R.3
Quick, J.4
Morris, J.5
-
53
-
-
0036892728
-
Polymorphism of roxifiban
-
Maurin MB, Vickery RD, Rabel SR, Rowe SM, Foris CM. 2002. Polymorphism of roxifiban. J Pharm Sci 91:2599-2604.
-
(2002)
J Pharm Sci
, vol.91
, pp. 2599-2604
-
-
Maurin, M.B.1
Vickery, R.D.2
Rabel, S.R.3
Rowe, S.M.4
Foris, C.M.5
-
54
-
-
0034858772
-
Characterization of two polymorphs of salmeterol xinofoate crystallized from supercritical fluids
-
Tong HH, Shekunov BY, York P, Chow AH. 2001. Characterization of two polymorphs of salmeterol xinofoate crystallized from supercritical fluids. Pharm Res 18:852-858.
-
(2001)
Pharm Res
, vol.18
, pp. 852-858
-
-
Tong, H.H.1
Shekunov, B.Y.2
York, P.3
Chow, A.H.4
-
55
-
-
0003730161
-
Polymorphs
-
Byrn S, Pfeiffer RR, Stowell RR, editors. West Lafayette, IN: SSCI, Inc.
-
Byrn S, Pfeifer RR, Stowell JG. 1999. Polymorphs. In: Byrn S, Pfeiffer RR, Stowell RR, editors. Solid-state chemistry of drugs. West Lafayette, IN: SSCI, Inc., pp 143-232.
-
(1999)
Solid-State Chemistry of Drugs
, pp. 143-232
-
-
Byrn, S.1
Pfeifer, R.R.2
Stowell, J.G.3
-
56
-
-
0019425151
-
The polymorphism of sulfathiazole
-
Lagas M, Lerk CF. 1981. The polymorphism of sulfathiazole. Int J Pharm 8:11-24.
-
(1981)
Int J Pharm
, vol.8
, pp. 11-24
-
-
Lagas, M.1
Lerk, C.F.2
-
57
-
-
0001497962
-
Determination of solubility of a metastable polymorph
-
Milosovich G. 1964. Determination of solubility of a metastable polymorph. J Pharm Sci 53:11-24.
-
(1964)
J Pharm Sci
, vol.53
, pp. 11-24
-
-
Milosovich, G.1
-
59
-
-
0032910069
-
Characterization of tolbutamide polymorphs (Burger's Forms II and IV) and polymorphic transition behavior
-
Kimura K, Hirayama F, Uekama K. 1999. Characterization of tolbutamide polymorphs (Burger's Forms II and IV) and polymorphic transition behavior. J Pharm Sci 88:385-391.
-
(1999)
J Pharm Sci
, vol.88
, pp. 385-391
-
-
Kimura, K.1
Hirayama, F.2
Uekama, K.3
-
60
-
-
0021686703
-
Thermodynamic studies of tolbutamide polymorphe
-
Rowe EL, Anderson BD. 1984. Thermodynamic studies of tolbutamide polymorphe. J Pharm Sci 73: 1673-1675.
-
(1984)
J Pharm Sci
, vol.73
, pp. 1673-1675
-
-
Rowe, E.L.1
Anderson, B.D.2
-
62
-
-
0026045869
-
Characterization of polymorphs of tranilast anhydrate and tranilast monhydrate when crystallized by two solvent change spherical crystallization techniques
-
Kawashima Y, Niwa T, Takeuchi H, Hino T, Itoh Y, Furuyama S. 1991. Characterization of polymorphs of tranilast anhydrate and tranilast monhydrate when crystallized by two solvent change spherical crystallization techniques. J Pharm Sci 80:472-478.
-
(1991)
J Pharm Sci
, vol.80
, pp. 472-478
-
-
Kawashima, Y.1
Niwa, T.2
Takeuchi, H.3
Hino, T.4
Itoh, Y.5
Furuyama, S.6
-
63
-
-
0028961823
-
WIN63843 polymorphs: Prediction of enantiotropy
-
Rocco WL, Swanson JR. 1995. WIN63843 polymorphs: prediction of enantiotropy. Int J Pharm 117:231-236.
-
(1995)
Int J Pharm
, vol.117
, pp. 231-236
-
-
Rocco, W.L.1
Swanson, J.R.2
-
64
-
-
0030576612
-
Influence of water activity in organic solvent + water mixture on the nature of the crystalline drug phase 2
-
Zhu H, Grant DJW. 1996. Influence of water activity in organic solvent + water mixture on the nature of the crystalline drug phase 2. Ampicillin Int J Pharm 139:33-43.
-
(1996)
Ampicillin Int J Pharm
, vol.139
, pp. 33-43
-
-
Zhu, H.1
Grant, D.J.W.2
-
65
-
-
0025942283
-
Polymorphism of carbamazepine: Solid-state studies on carbamazepine dihydrate
-
Dugue J, Ceolin R, Rouland JC, Lepage F. 1991. Polymorphism of carbamazepine: Solid-state studies on carbamazepine dihydrate. Pharm Acta Helv 66:307-310.
-
(1991)
Pharm Acta Helv
, vol.66
, pp. 307-310
-
-
Dugue, J.1
Ceolin, R.2
Rouland, J.C.3
Lepage, F.4
-
66
-
-
0021040213
-
Physical characterization of erythromycin dihydrate, anhydrate and amorphous solid and their dissolution properties
-
Fukumori Y, Fukuda T, Yamamoto Y, Shigitani Y, Hanyu Y, Takeuchi Y, Sato N. 1983. Physical characterization of erythromycin dihydrate, anhydrate and amorphous solid and their dissolution properties. Chem Pharm Bull 31:4029-4039.
-
(1983)
Chem Pharm Bull
, vol.31
, pp. 4029-4039
-
-
Fukumori, Y.1
Fukuda, T.2
Yamamoto, Y.3
Shigitani, Y.4
Hanyu, Y.5
Takeuchi, Y.6
Sato, N.7
-
68
-
-
0344012503
-
Structural characterization, physicochemical properties, and thermal stability of three crystal forms of nifedipine
-
Caira KC, Robbertse Y, Bergh JJ, Song M, De Villiers MM. 2003. Structural characterization, physicochemical properties, and thermal stability of three crystal forms of nifedipine. J Pharm Sci 92:2519-2533.
-
(2003)
J Pharm Sci
, vol.92
, pp. 2519-2533
-
-
Caira, K.C.1
Robbertse, Y.2
Bergh, J.J.3
Song, M.4
De Villiers, M.M.5
-
69
-
-
0020700048
-
A thermodynamic study of the solubility of theophylline and its hydrate
-
Fokkens JG, van Amelsfoort JGM, de Blaey CJ, de Kruif CG, Wilting J. 1983. A thermodynamic study of the solubility of theophylline and its hydrate. Int J Pharm 14:79-92.
-
(1983)
Int J Pharm
, vol.14
, pp. 79-92
-
-
Fokkens, J.G.1
Van Amelsfoort, J.G.M.2
De Blaey, C.J.3
De Kruif, C.G.4
Wilting, J.5
-
70
-
-
0029152059
-
Solid-state characterization of dehydroepiandrosterone
-
Chang LC, Caira MR, Guillory JK. 1995. Solid-state characterization of dehydroepiandrosterone. J Pharm Sci 84:1169-1179.
-
(1995)
J Pharm Sci
, vol.84
, pp. 1169-1179
-
-
Chang, L.C.1
Caira, M.R.2
Guillory, J.K.3
-
71
-
-
0027771548
-
Solid-state NMR and IR for the analysis of pharmaceutical solids: Polymorphs of fosinopril sodium
-
Brittain HG, Morris KR, Bugay DE, Thakur AB, Serajuddin ATM. 1993. Solid-state NMR and IR for the analysis of pharmaceutical solids: polymorphs of fosinopril sodium. J Pharm Biomed Anal 11: 1063-1069.
-
(1993)
J Pharm Biomed Anal
, vol.11
, pp. 1063-1069
-
-
Brittain, H.G.1
Morris, K.R.2
Bugay, D.E.3
Thakur, A.B.4
Serajuddin, A.T.M.5
-
72
-
-
0031923295
-
Crystal forms of piroxicam pivalate: Preparation and characterization of two polymorphs
-
Giordano F, Gazzaniga A, Moyano JR, Ventura P, Zanol M, Peveri T, Carima L. 1998. Crystal forms of piroxicam pivalate: Preparation and characterization of two polymorphs. J Pharm Sci 87:333-337.
-
(1998)
J Pharm Sci
, vol.87
, pp. 333-337
-
-
Giordano, F.1
Gazzaniga, A.2
Moyano, J.R.3
Ventura, P.4
Zanol, M.5
Peveri, T.6
Carima, L.7
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